metformin hydrochloride
Generic: metformin hydrochloride
Labeler: aurobindo pharma limitedDrug Facts
Product Profile
Brand Name
metformin hydrochloride
Generic Name
metformin hydrochloride
Labeler
aurobindo pharma limited
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
metformin hydrochloride 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
59651-854
Product ID
59651-854_472751ac-42ed-4484-bb92-46b61e39d8ea
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077095
Listing Expiration
2026-12-31
Marketing Start
2024-03-29
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
59651854
Hyphenated Format
59651-854
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
metformin hydrochloride (source: ndc)
Generic Name
metformin hydrochloride (source: ndc)
Application Number
ANDA077095 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 100 TABLET, FILM COATED in 1 BOTTLE (59651-854-01)
- 500 TABLET, FILM COATED in 1 BOTTLE (59651-854-05)
- 4500 TABLET, FILM COATED in 1 BOTTLE (59651-854-45)
- 50 TABLET, FILM COATED in 1 BOTTLE (59651-854-50)
- 60 TABLET, FILM COATED in 1 BOTTLE (59651-854-60)
- 300 TABLET, FILM COATED in 1 BOTTLE (59651-854-79)
- 90 TABLET, FILM COATED in 1 BOTTLE (59651-854-90)
- 1000 TABLET, FILM COATED in 1 BOTTLE (59651-854-99)
Packages (8)
59651-854-01
100 TABLET, FILM COATED in 1 BOTTLE (59651-854-01)
59651-854-05
500 TABLET, FILM COATED in 1 BOTTLE (59651-854-05)
59651-854-45
4500 TABLET, FILM COATED in 1 BOTTLE (59651-854-45)
59651-854-50
50 TABLET, FILM COATED in 1 BOTTLE (59651-854-50)
59651-854-60
60 TABLET, FILM COATED in 1 BOTTLE (59651-854-60)
59651-854-79
300 TABLET, FILM COATED in 1 BOTTLE (59651-854-79)
59651-854-90
90 TABLET, FILM COATED in 1 BOTTLE (59651-854-90)
59651-854-99
1000 TABLET, FILM COATED in 1 BOTTLE (59651-854-99)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "472751ac-42ed-4484-bb92-46b61e39d8ea", "openfda": {"unii": ["786Z46389E"], "rxcui": ["861004", "861007", "861010"], "spl_set_id": ["fc466c46-abaa-4675-aef2-4b1a1adfd912"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (59651-854-01)", "package_ndc": "59651-854-01", "marketing_start_date": "20240329"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (59651-854-05)", "package_ndc": "59651-854-05", "marketing_start_date": "20240329"}, {"sample": false, "description": "4500 TABLET, FILM COATED in 1 BOTTLE (59651-854-45)", "package_ndc": "59651-854-45", "marketing_start_date": "20240329"}, {"sample": false, "description": "50 TABLET, FILM COATED in 1 BOTTLE (59651-854-50)", "package_ndc": "59651-854-50", "marketing_start_date": "20240329"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (59651-854-60)", "package_ndc": "59651-854-60", "marketing_start_date": "20240329"}, {"sample": false, "description": "300 TABLET, FILM COATED in 1 BOTTLE (59651-854-79)", "package_ndc": "59651-854-79", "marketing_start_date": "20240329"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (59651-854-90)", "package_ndc": "59651-854-90", "marketing_start_date": "20240329"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (59651-854-99)", "package_ndc": "59651-854-99", "marketing_start_date": "20240329"}], "brand_name": "Metformin Hydrochloride", "product_id": "59651-854_472751ac-42ed-4484-bb92-46b61e39d8ea", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "59651-854", "generic_name": "Metformin Hydrochloride", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA077095", "marketing_category": "ANDA", "marketing_start_date": "20240329", "listing_expiration_date": "20261231"}